Evidence map›Paper›PMID 34803516›Full record

ArticleBiometrika2021

Covariate adaptive familywise error rate control for genome-wide association studies.

Huijuan Zhou, Xianyang Zhang, Jun Chen

Abstract read
In one paragraph

Article in Biometrika, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

3 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

3 authors.

Huijuan ZhouInstitute of Statistics and Big Data, Renmin University of China, Beijing 100872, China.
Xianyang ZhangDepartment of Statistics, Texas A&M University, College Station, Texas 77843, U.S.A.
Jun ChenDivision of Biomedical Statistics and Informatics, Mayo Clinic, 200 First St. SW, Rochester, Minnesota 55905, U.S.A.

Funding

Methods for Analysis of Genomic Data with Auxiliary InformationR21HG011662 · NHGRI · MAYO CLINIC ROCHESTER · PI CHEN, JUN, ZHANG, XIANYANG · 2021 to 2022
$434k
Medical Research Council MC_PC_17228Medical Research Council MC_QA137853NHGRI NIH HHS R21 HG011662
6 · The paper itself

Abstract

The familywise error rate has been widely used in genome-wide association studies. With the increasing availability of functional genomics data, it is possible to increase detection power by leveraging these genomic functional annotations. Previous efforts to accommodate covariates in multiple testing focused on false discovery rate control, while covariate-adaptive procedures controlling the familywise error rate remain underdeveloped. Here, we propose a novel covariate-adaptive procedure to control the familywise error rate that incorporates external covariates which are potentially informative of either the statistical power or the prior null probability. An efficient algorithm is developed to implement the proposed method. We prove its asymptotic validity and obtain the rate of convergence through a perturbation-type argument. Our numerical studies show that the new procedure is more powerful than competing methods and maintains robustness across different settings. We apply the proposed approach to the UK Biobank data and analyse 27 traits with 9 million single-nucleotide polymorphisms tested for associations. Seventy-five genomic annotations are used as covariates. Our approach detects more genome-wide significant loci than other methods in 21 out of the 27 traits.

Indexed as

EM algorithmExternal covariateFamilywise error rateMultiple testing

Identifiers

PMID34803516
PMCPMC8598971

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.